GM2-gangliosidosis-Reference-Cited by-同舟云学术

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GM2-gangliosidosis

Published:1990-01 Issue:2 Volume:92 Page:143-148
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Praamstra P.,Wevers R.A.,Gabreëls F.J.M.,Rotteveel J.J.,Renier W.O.,Sengers R.C.A.,Lamers K.J.B.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Surgery

Reference15 articles.

1. Tay-Sachs disease: generalized absence of a β-D-N-acetylhexosaminidase component;Okada;Science,1969

2. The Gangliosidoses;O'Brien,1984

3. Juvenile GM2-gangliosidosis: Biochemical and ultrastructural studies on a new variant of Tay Sachs disease;Menkes;Arch Neurol,1971

4. Late onset GM2- gangliosidosis. Clinical, pathological, and biochemical studies on eight patients;Brett;Arch Dis Child,1973

5. Clinical and genetic variations in the syndrome of adult GM2-gangliosidosis resulting from hexosaminidase A deficiency;Argov;Ann Neurol,1984

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Infantile Sandhoff Disease: Unusual presentation;Medical Journal Armed Forces India;2016-12

2. Infantile Sandhoff's disease;South African Journal of Radiology;2009-08-20

3. GM2 Gangliosidosis;Magnetic Resonance of Myelin, Myelination, and Myelin Disorders;1995

4. A nursing challenge: Adult-Onset Tay-Sachs disease;Archives of Psychiatric Nursing;1991-12

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